Canonical Allele Identifier: CA1329111864

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219210715T= , CM000664.2:g.219210715T= GRCh38
NC_000002.11:g.220075437T= , CM000664.1:g.220075437T= GRCh37
NC_000002.10:g.219783681T= NCBI36
NG_032110.1:g.13276A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.2252A= (ABCB6) MANE Select ENSP00000265316.3:p.Asp751=
ENST00000295750.5:c.2114A= (ABCB6) ENSP00000295750.5:p.Asp705=
ENST00000265316.7:c.2252A= (ABCB6) ENSP00000265316.3:p.Asp751=
ENST00000295750.4:c.1795A= (ABCB6)
ENST00000443805.1:c.240A= (ABCB6)
ENST00000446716.5:c.4802A= (ATG9A)
ENST00000485773.5:n.284A= (ABCB6)
ENST00000487380.5:n.325A= (ABCB6)
ENST00000492543.1:n.802A= (ABCB6)
ENST00000497882.5:n.2565A= (ABCB6)
NM_005689.2:c.2252A= (ABCB6) NP_005680.1:p.Asp751=
NM_001349828.1:c.2114A= (ABCB6) NP_001336757.1:p.Asp705=
NM_005689.3:c.2252A= (ABCB6) NP_005680.1:p.Asp751=
NM_005689.4:c.2252A= (ABCB6) MANE Select NP_005680.1:p.Asp751=
NM_001349828.2:c.2114A= (ABCB6) NP_001336757.1:p.Asp705=